Biocompatible Nanoparticles Intercalated with Anticancer Drug for Target Delivery: Pharmacokinetic and Biodistribution Study

被引:89
作者
Choi, Soo-Jin [1 ,2 ,3 ]
Oh, Jae-Min [1 ,2 ,4 ]
Choy, Jin-Ho [1 ,2 ]
机构
[1] Ewha Womans Univ, Dept Bioinspired Sci, Div Nano Sci BK21, Ctr Intelligent Nanobio Mat, Seoul 120750, South Korea
[2] Ewha Womans Univ, Dept Chem & Nano Sci, Seoul 120750, South Korea
[3] Seoul Womens Univ, Dept Food Sci & Technol, Seoul 139774, South Korea
[4] Yonsei Univ, Dept Chem & Med Chem, Wonju 220710, Gangwon Do, South Korea
关键词
Biocompatibility; Anticancer Drug; Layered Double Hydroxide; Pharmacokinetics; Biodistribution; LAYERED DOUBLE HYDROXIDES; NANOHYBRIDS;
D O I
10.1166/jnn.2010.1415
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed new hybrid systems consisting of anticancer drugs such as methotrexate (MTX) or 5-fluorouracil (5-FU) and two-dimensional inorganic delivery carrier like layered double hydroxide (LDH). Such an inorganic vector with biocompatible metal ions can be used to overcome toxicity, immunogenecity and poor integration capacity, which are critical problems caused by conventional viral vectors, cationic liposomes and polymers. Moreover, the intercellular mechanism of LDH nanoparticles is primarily related to clathrin-mediated endocytosis, resulting in effective delivery and eventually enhancing drug efficacy. In this report, the effect of LDH intercalated with 5-Fu (5-Fu-LDH) was evaluated in whole animal by studying pharmacokinetic behavior and tissue distribution. The results showed that 5-Fu-LDH exhibited favorable blood clearance profiles compared to free 5-Fu, such as sustained drug release, prolonged drug half-life, and increased drug accumulation in target tumor tissue. Furthermore, LDH nanoparticles were rapidly excreted from the body and not accumulated in the organs after administration as 5-Fu-LDH. Therefore, the hybrid system can be promising anticancer chemotherapy agent for tumor targeting with biocompatibility.
引用
收藏
页码:2913 / 2916
页数:4
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